Evidence map›Paper›PMID 35172128›Full record

ArticleCurrent biology : CB2022

Dissociable oscillatory theta signatures of memory formation in the developing brain.

Elizabeth L Johnson, Qin Yin, Nolan B O'Hara, Lingfei Tang, Jeong-Won Jeong, Eishi Asano, Noa Ofen

Abstract read
In one paragraph

Article in Current biology : CB, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Oxytocin selectively biases sensory-prefrontal communication through network-level suppression and theta coupling.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  4. Quantum-inspired entanglement between collaborating brains during human memory encoding.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  6. Review
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  11. Cortical and white matter substrates supporting visuospatial working memory.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Elizabeth L JohnsonLife-Span Cognitive Neuroscience Program, Institute of Gerontology and Merrill Palmer Skillman Institute, Wayne State University, Detroit, MI 48202, USA; Departments of Medical Social Sciences and Pediatrics, Northwestern University, Chicago, IL 60611, USA; Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720, USA. Electronic address: eljohnson@northwestern.edu.
Qin YinLife-Span Cognitive Neuroscience Program, Institute of Gerontology and Merrill Palmer Skillman Institute, Wayne State University, Detroit, MI 48202, USA; Department of Psychology, Wayne State University, Detroit, MI 48202, USA.
Nolan B O'HaraTranslational Neuroscience Program, Wayne State University, Detroit, MI 48201, USA.
Lingfei TangLife-Span Cognitive Neuroscience Program, Institute of Gerontology and Merrill Palmer Skillman Institute, Wayne State University, Detroit, MI 48202, USA; Department of Psychology, Wayne State University, Detroit, MI 48202, USA.
Jeong-Won JeongTranslational Neuroscience Program, Wayne State University, Detroit, MI 48201, USA; Departments of Pediatrics and Neurology, Children's Hospital of Michigan, Wayne State University, Detroit, MI 48201, USA.
Eishi AsanoTranslational Neuroscience Program, Wayne State University, Detroit, MI 48201, USA; Departments of Pediatrics and Neurology, Children's Hospital of Michigan, Wayne State University, Detroit, MI 48201, USA.
Noa OfenLife-Span Cognitive Neuroscience Program, Institute of Gerontology and Merrill Palmer Skillman Institute, Wayne State University, Detroit, MI 48202, USA; Department of Psychology, Wayne State University, Detroit, MI 48202, USA; Translational Neuroscience Program, Wayne State University, Detroit, MI 48201, USA. Electronic address: noa.ofen@wayne.edu.

Funding

Functional brain mapping in pediatric neurosurgeryR01NS064033 · NINDS · WAYNE STATE UNIVERSITY · PI EISHI ASANO · 2009 to 2026
$5.7M
DEVELOPMENT OF MEMORY NETWORKS IN CHILDRENR01MH107512 · NIMH · WAYNE STATE UNIVERSITY · PI Noa Ofen · 2016 to 2026
$5.0M
Novel DWI Methods to Minimize Postoperative Deficits in Pediatric Epilepsy Surgery.R01NS089659 · NINDS · WAYNE STATE UNIVERSITY · PI JEONG, JEONG-WON · 2015 to 2025
$3.7M
Measuring Electrical Activity from the Human Brain to Predict Memory Formation and Behavior Across the LifespanR00NS115918 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JOHNSON, ELIZABETH · 2022 to 2024
$843k
NIMH NIH HHS R01 MH107512NINDS NIH HHS R00 NS115918NINDS NIH HHS R01 NS064033NINDS NIH HHS R01 NS089659
6 · The paper itself

Abstract

Understanding complex human brain functions is critically informed by studying such functions during development. Here, we addressed a major gap in models of human memory by leveraging rare direct electrophysiological recordings from children and adolescents. Specifically, memory relies on interactions between the medial temporal lobe (MTL) and prefrontal cortex (PFC), and the maturation of these interactions is posited to play a key role in supporting memory development. To understand the nature of MTL-PFC interactions, we examined subdural recordings from MTL and PFC in 21 neurosurgical patients aged 5.9-20.5 years as they performed an established scene memory task. We determined signatures of memory formation by comparing the study of subsequently recognized to forgotten scenes in single trials. Results establish that MTL and PFC interact via two distinct theta mechanisms, an ∼3-Hz oscillation that supports amplitude coupling and slows down with age and an ∼7-Hz oscillation that supports phase coupling and speeds up with age. Slow and fast theta interactions immediately preceding scene onset further explained age-related differences in recognition performance. Last, with additional diffusion imaging data, we linked both functional mechanisms to the structural maturation of the cingulum tract. Our findings establish system-level dynamics of memory formation and suggest that MTL and PFC interact via increasingly dissociable mechanisms as memory improves across development.

Indexed as

Prefrontal CortexTemporal LobeAdolescentChildHumansMagnetic Resonance ImagingNerve NetRecognition, PsychologyTheta Rhythmbrain developmentcognitive developmentdiffusion tractographyelectrocorticographyepisodic memorymedial temporal lobeprefrontal cortextheta oscillations

Identifiers

PMID35172128
PMCPMC9007830

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.